Related gene-specific medical variations for Gene (Select 3364) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2569114	NM_004507.4(HUS1):c.28G>T (p.Gly10Trp)	HUS1, LOC129998418 (G10W)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2270322	NM_004507.4(HUS1):c.38T>G (p.Leu13Arg)	HUS1, LOC129998418 (L13R)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 771411	NM_004507.4(HUS1):c.51A>G (p.Thr17=)	HUS1, LOC129998418	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GBenign

Format

Sort by

Choose Destination